NL-OMON39302已完成2 期
Memantine Add-On Therapy to Clozapine - MAOTC
GGZ NH0 个研究点目标入组 52 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 52
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99(—)
入选标准
- •Eligible for the study are outpatients, both sexes, age 18 to 60, meeting DSM-IV criteria for schizophrenia, based on the definitions in the Mini International Neuropsychiatric Interview Plus (MINI-Plus) with persistent residual psychopathology, failing to achieve the remission criteria, after adequate treatment with clozapine for at least 6 months. Before the start of the study clozapine plasma concentration has been at least 350 ng/ml for 12 weeks or has not reached 350 ng/ml due to intolerability. Remission defined as simultaneous ratings of mild or less (<= 3 points) on 8 of the PANSS items evaluating the core symptoms of schizophrenia (P1 delusions, G9 unusual thought content, P3 hallucinatory behaviour, P2 conceptual disorganisation, G5 mannerisms and posturing, N1 blunted affect, N4 passive or apathetic social withdrawal, N6 lack of spontaneity and flow of conversation) (Os van and Kahn, 2007). Patients should be able to understand the study information and procedures and give informed consent. All participants fulfilling the inclusion and not fulfilling the exclusion criteria may, after a detailed description by a doctor and the written declaration of informed consent on an according form, participate in the study.
排除标准
- •- Pregnancy.
- •- Lactating women.
- •- Female subjects without adequate contraception.
- •- Known hypersensitivity to memantine or ingredients used in this tablet.
- •- Uncontrolled epilepsy.
- •- Recent myocardial infarction.
- •- Uncontrolled hypertension.
- •- Renal insufficiency (GFR less than 30 ml/min).
- •- Severe liver failure (ASAT 175 U/l and/or ALAT 225 U/l in men and 175 U/l in women).
- •- Lactose intolerance.
- •- Co-medication with NMDA-antagonists such as amantadine, ketamine, dextromethorphan.
- •-Co-medication with glutamate antagonists such as lamotrigine and topiramate.
- •- Extremely ill patients (Global Assessment of Functioning [GAF] <= 20), who are not reliably able to give their informed consent.
- •- Moderate or severe Alzheimer*s disease.
研究者
相似试验
进行中(未招募)
不适用
Memantine as an adjunctive therapy to ongoing clozapine treatment: a proof-of-concept studyEUCTR2011-003466-33-NLMental Health Services North Holland North
已完成
2 期
Memantine as an adjunctive therapy to ongoing clozapine treatment: a proof-of-concept study and follow-up studyISRCTN14760638Mental Health Service Organisation North Holland North, Community Mental Health Division52
已完成
4 期
Memantine as Adjunctive Therapy for Schizophrenia Negative SymptomsSchizophreniaNCT00757978Hospital de Clinicas de Porto Alegre22
尚未招募
Unknown
A comparative clinical experiment of mirtazapine and amitriptyline in India on patients with recurring symptoms of an upset stomach that have no obvious causeCTRI/2024/01/061596Indian Council of Medical Research (ICMR)
已完成
4 期
Mirtazapine add-on therapy in the treatment of schizophrenia with atypical neuroleptics: A double-blind, randomised, placebo controlled trialMental Health - SchizophreniaSchizophreniaACTRN12605000577617niversity of Melbourne40
